首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   660435篇
  免费   40148篇
  国内免费   950篇
耳鼻咽喉   8899篇
儿科学   20868篇
妇产科学   16957篇
基础医学   106458篇
口腔科学   19649篇
临床医学   52860篇
内科学   126180篇
皮肤病学   16203篇
神经病学   48223篇
特种医学   21920篇
外国民族医学   63篇
外科学   93728篇
综合类   9190篇
一般理论   142篇
预防医学   56415篇
眼科学   16064篇
药学   52011篇
中国医学   1640篇
肿瘤学   34063篇
  2021年   5386篇
  2019年   6072篇
  2018年   9500篇
  2017年   6506篇
  2016年   6942篇
  2015年   7717篇
  2014年   9600篇
  2013年   14928篇
  2012年   22328篇
  2011年   24159篇
  2010年   13181篇
  2009年   11343篇
  2008年   21729篇
  2007年   23394篇
  2006年   23216篇
  2005年   22263篇
  2004年   21355篇
  2003年   20214篇
  2002年   19755篇
  2001年   28063篇
  2000年   29524篇
  1999年   23907篇
  1998年   6061篇
  1997年   5118篇
  1996年   5444篇
  1995年   4977篇
  1992年   17560篇
  1991年   17961篇
  1990年   18071篇
  1989年   17202篇
  1988年   15907篇
  1987年   15671篇
  1986年   14842篇
  1985年   14134篇
  1984年   10477篇
  1983年   8991篇
  1979年   10417篇
  1978年   7533篇
  1977年   6439篇
  1976年   6234篇
  1975年   7146篇
  1974年   8566篇
  1973年   8098篇
  1972年   7922篇
  1971年   7611篇
  1970年   7032篇
  1969年   6803篇
  1968年   6504篇
  1967年   5851篇
  1966年   5220篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
51.
52.
53.
Mitochondria are known primarily as the location of the electron transport chain and energy production in cells. More recently, mitochondria have been shown to be signaling centers for apoptosis and inflammation. Reactive oxygen species (ROS) generated as by-products of the electron transport chain within mitochondria significantly impact cellular signaling pathways. Because of the toxic nature of ROS, mitochondria possess an antioxidant enzyme, superoxide dismutase 2 (SOD2), to neutralize ROS. If mitochondrial antioxidant enzymes are overwhelmed during severe infections, mitochondrial dysfunction can occur and lead to multiorgan failure or death. Pseudomonas aeruginosa is an opportunistic pathogen that can infect immunocompromised patients. Infochemicals and exotoxins associated with P. aeruginosa are capable of causing mitochondrial dysfunction. In this work, we describe the roles of SOD2 and mitochondrial ROS regulation in the zebrafish innate immune response to P. aeruginosa infection. sod2 is upregulated in mammalian macrophages and neutrophils in response to lipopolysaccharide in vitro, and sod2 knockdown in zebrafish results in an increased bacterial burden. Further investigation revealed that phagocyte numbers are compromised in Sod2-deficient zebrafish. Addition of the mitochondrion-targeted ROS-scavenging chemical MitoTEMPO rescues neutrophil numbers and reduces the bacterial burden in Sod2-deficient zebrafish. Our work highlights the importance of mitochondrial ROS regulation by SOD2 in the context of innate immunity and supports the use of mitochondrion-targeted ROS scavengers as potential adjuvant therapies during severe infections.  相似文献   
54.
55.
56.
57.

Background

Since recent reports have shown that (-)-Epigallocatechin-3-gallate (EGCG) could be used for treating proliferative and inflammatory disorders, we explored its use for the management of corneal chemical burns.

Materials and methods

Initially, EGCG was assayed on the rabbit corneal epithelial cell line RCE1(5T5) to establish the best testing conditions, and to avoid unwanted outcomes in the experimental animals. Then, we studied its effects on cell proliferation, cell cycle progression and cell differentiation. Afterwards, we instilled EGCG in experimental grade II corneal alkali burns in mice, three times a day up to 21 days, and evaluated by slit lamp examination and histological sections of corneal epithelial, corneal endothelial and stromal edema, as well as the presence of inflammatory cells and neovascularization.

Results

EGCG reduced cell growth and led to a decline in the proportion of proliferative cells in a concentration dependent manner. At 10 μM, EGCG promoted cell differentiation, an effect not related with apoptosis or cytotoxicity. When 10 μM EGCG was instilled in corneal alkali burns in mice three times a day up to 21 days, EGCG significantly reduced corneal opacity and neovascularization. The improved clinical appearance of the cornea was associated to a controlled epithelial growth; epithelial morphology was similar to that observed in normal epithelium and contrasted with the hyperproliferative, desquamating epithelium observed in control burn wounds. EGCG reduced corneal, stromal and endothelial edema, and wound inflammation.

Conclusion

This work constitutes the first evidence for the use of EGCG in the acute phase of a corneal alkali burn, representing a possible novel alternative to improve patient outcomes as an add-on therapy.  相似文献   
58.
59.
60.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号